A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5828098



Internal ID22603033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:145567172..145573895hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg386724
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17459359, nssv17462786
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5828098
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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